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/ Not yet recruitingPhase 1/2 A Multi-centre, Phase 1/2, Randomised, Double-blind, Placebo Controlled Study With an Optional Open-label Extension to Evaluate the Safety, Tolerability, Efficacy, and Pharmacodynamics of PLL001 for the Treatment of ALS
FIH, Phase 1/2, multi-centre, randomised, double-blind, placebo controlled study with an optional open-label dosing extension to assess the safety, tolerability, efficacy, and Pharmacodynamics (PD) of single or multiple (up to 48 weeks QD) subcutaneous (SC) doses of PLL001 compared to placebo in subjects diagnosed with ALS.
100 Clinical Results associated with PLL-Therapeutics
0 Patents (Medical) associated with PLL-Therapeutics
100 Deals associated with PLL-Therapeutics
100 Translational Medicine associated with PLL-Therapeutics